NM_001172811.1:c.*105G>T

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  2. NM_001172811.1:c.*105G>T

HGVS Expressions

  • NM_001172811.1:c.*105G>T
  • NP_001166282.1:p.?
  • NC_000008.11:g.117172786G>T

Associated Genes

Solute Carrier Family 30 (Zinc Transporter), Member 8
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CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

3802177

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
611145.G.1Lebanon1069BenignAlmawi et al. 2013 Among subjects with 995 T2DM patients an...
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Contributors

  • Sami Bizzari: 11.03.2021

Edit History

  • Sami Bizzari: 14.03.2021
  • Sami Bizzari: 11.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.